Vasculitis Flashcards

1
Q

what is vasculitis

A

inflammation of blood vessels

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2
Q

vessels changes that occur in vasculitis

A

vessel wall thickening vessel wall stenosis occlusion of vessels – infarction

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3
Q

what are the two types of large vessel vasculitis

A
  1. Giant cell arteritis 2. Takayasu arteritis
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4
Q

what age group does giant cell arteritis present in

A

females > 50 years old

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5
Q

what condition do 50% of people with giant cell arteritis also have

A

polymyalgia reumatica

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6
Q

Giant cell arteritis affects which vessels

A

cranial branches of arteries from aortic arch

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7
Q

symptoms of giant cell arteritis

A

unilateral throbbing headache scalp tenderness jaw claudication blurred vision systemic: fever, malaise

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8
Q

what is a transient painless loss of vision in giant cell arteritis called

A

amaurosis fugax

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9
Q

what is seen on biopsy in giant cell arteritis

A

multinucleated giant cells - can have skip lesions

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10
Q

treatment of giant cell arteritis

A

prednisolone 40mg - 60mg if ocular involvement

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11
Q

what age group does takayasu’s arteritis present in

A

females <40 more common in asians

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12
Q

duplex ultrasound of temporal artery in GCA shows what?

A

halo sign

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13
Q

signs of takayasu’s arteritis

A

unequal BP in arms bruits aortic regurgitation limi claudication hypertension

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14
Q

treatment of takayasu’s arteritis

A

prednisolone 40-60mg

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15
Q

what is henoch schonlein purpura

A

IgA vasculitis - commonly affects children

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16
Q

presentation of henoch schonlein purpura

A

pupura - buttocks/lower limbs joint pain abdominal pain renal involvement - IgA nephritis

17
Q

treatment of henoch schonlein purpura

A

supportive

18
Q

what is polyarteritis nodosa

A

medium vessel arteritis associated with Hepatitis B

19
Q

how it takayasu’s arteritis diagnosed

A

CT / MRI angiography

20
Q

general symptoms of small vessel vasculitis

A

pupura - non blanching rash

arthritis

renal impairment

GI disturbance

neuropathy

21
Q

p-ANCA is associated with which types of vasculitis

A

eosinophilic granulomatosis with polyangitis (EGPA)

  • Peviously known as Churg Strauss

microscopic polyangitis

22
Q

what are p-ANCA antibodies also known as

A

MPO

23
Q

Features of EGPA

A

Late onset asthma, rhinitis

raised eosinophil count

24
Q

differences between EGPA and microscopic polyangitis

A

both p-ANCA +ve

  • absence of eosinophilia + granulomas in microscopic polyangitis
  • sparing of upper airways in microscopic polyangitis
  • glomerulonephritis in 90% of microscopic polyangitis, less common EGPA
25
Q

c-ANCA is associated with which type of vasculitis

A

Granulomatosis with polyangitis (GPA)

  • previously knoen as Wegners syndrome
26
Q

features of GPA

A

Nose bleeds, recurrent sinusitis, deafness, nasal crusting

SOB + cough - cavitating opacities on CXR

27
Q

treatment of small vessel vasculitis

A

IV steroids + cyclophosphamide

28
Q

what is kawasaki disease

A

medium vessel vasculitis that affects young children, typically under 5

29
Q

features of kawasaki disease

A
  • fever >5 days
  • blanching rash
  • conjunctivitis
  • strawberry tongue (red tongue)
  • red palms/soles than peel
30
Q

serious complication of kawasaki disease

A

coronary aneurysms

31
Q

treament of kawasaki disease

A

high dose aspirin + IV immunoglobulins

32
Q

what is Behcets

A

systemic vasculitis

  • presents with arthritis, genital ulceration + eye inflammation
  • young men, typically mediterranean/asian